Neomycin

It is used in treating such conditions as acute otitis externa in dogs and to a lesser degree, chronic otitis externa in dogs. It also is effective in treating anal gland infections and moist dermatitis in the dog and is a useful dressing for minor cuts, lacerations, abrasions, and post-surgical therapy in the dog. It may also be used following amputation of dewclaw, tails and claws, following ear trimming and castrating operations.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

For topical dermatological use. Use either ointment for anti-inflammatory, antipruritic, antifungal, and antibacterial treatment of superficial bacterial infections, and for dermatologic disorders characterized by inflammation and dry or exudative dermatitis, particularly associated with bacterial or candidal (Candida albicans) infections.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

Topically: Use either ointment in dogs and cats for anti-inflammatory, antipruritic, antifungal, and antibacterial treatment of superficial bacterial infections, and for dermatologic disorders characterized by inflammation and dry or exudative dermatitis, particularly associated with bacterial or candidal (Candida albicans) infections.

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derma-Vet Cream

The drug is used in the relief of pruritus and inflammation associated with superficial acute and chronic dermatoses in dogs. It is used in the treatment of such conditions as allergic and acute moist dermatoses and nonspecific dermatoses in dogs. It is used in the treatment of wound infections in dogs.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-synalar Cream

Treatment of the inflammation, edema, and secondary bacterial infections associated with topical ophthalmological conditions of the eye such as corneal injuries, incipient pannus, superficial keratitis, conjunctivitis, acute nongranulomatous anterior uveitis, kerato- conjunctivitis, and blepharitis.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Ophthalmic Solution

The drug is recommended for use in superficial ocular inflammations or infections limited to the conjunctiva or the anterior segment of the eye of dogs, such as those associated with allergic reactions or gross irritants.

All topical ophthalmic preparations containing corticosteroids with or without an antimicrobial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until the infection is under control and corneal regeneration is well underway. For use only by or on the order of a licensed veterinarian.

Hydeltrone Ointment

For the treatment of bacterial infections associated with topical ophthalmological conditions such as corneal injuries, superficial keratitis, conjunctivitis, keratoconjunctivitis, and blepharitis.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Opthakote Ophthalmic

It is indicated for treating acute otitis externa and, to a lesser degree, chronic otitis externa in dogs. In treatment of ear canker and other inflammatory conditions of the external ear canal.

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® with Tetracaine

Otitis, cysts, and anal gland infections: Use petrolatum base ointment in dogs for the treatment of acute and chronic otitis and interdigital cysts, and in dogs for anal gland infections.

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Panolog® Ointment

The drug is intended for use in dogs for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycane Ophthalmic Ointment

Treatment of summer eczema, atopic dermatitis, interdigital eczema and otitis externa caused by bacteria susceptible to neomycin, penicillin, and polymyxin B.

For use in dogs only. Shake drug thoroughly and clean lesion before using. If redness, irritation, or swelling persists or increases, discontinue use and reevaluate diagnosis. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Forte Topical® Ointment

For treating infections, allergic, and traumatic keratitis, conjunctivitis, acute otitis externa and, to a lesser degree, chronic otitis externa in dogs.

All topical ophthalmic preparations containing corticosteroids, with or without an antimicrobial agent, are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non-susceptible organisms or to prolonged use on antibiotic-containing preparations resulting in overgrowth of non-susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® Sterile Ointment

The drug is indicated for treating infectious allergic and traumatic keratitis and conjunctivitis, otitis externa, and chronic otitis externa in dogs.

All topical ophthalmic preparations containing corticosteroids with or without an anti-microbial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Delta Cortef® Sterile Solution

For treating acute otitis externa and as adjunctive therapy in management of chronic otitis externa. Also for treating moist dermatitis in dogs.

Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Liquisone F with Cerumene

For infected anal glands and cystic areas. Use petrolatum base ointment for the treatment of interdigital cysts, and for anal gland infections.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derma 4 Ointment

The drug is used in dogs to control bacterial diarrhea caused by organisms susceptible to neomycin and to reduce smooth muscle contractions.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Jenomycin Tablets

The drug is recommended for use as an aid in the treatment of bacterial, mycotic, and inflammatory dermatoses and otitis externa in dogs.

For use only by or on order of a licensed veterinarian.

Tresaderm Dermatologic Solution

Treatment of superficial bacterial infections of the eyelid and conjunctiva of dogs and cats when due to susceptible organisms.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Bac-Neo-Poly Ophthalmic Ointment

Administer to dogs for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Neomycin is not for use parenterally in food-producing animals because of prolonged residues in edible tissues. Labeling shall bear an appropriate expiration date. For use by or on the order of a licensed veterinarian.

Biosol® Sterile Solution

For treatment of dogs in which infectious bacterial gastroenteritis is associated with emotional stress.

Do not continue medication longer than 5 days. Overdosage or prolonged administration may produce nephrotoxicity as manifested by albuminuria, presence of granular casts and depressed urinary output. If it is desirable to administer a vasoconstrictor, norepinephrine is the drug of choice. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Darbazine Spansule Capsule No.1

For otic use. Use petrolatum base ointment for the treatment of acute and chronic otitis.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

Treating acute or chronic conjunctivitis caused by susceptible organisms.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Bacitracin-Neomycin-Polymyxin with Hydrocortisone Acetate Ophthalmic Ointment

For topical dermatological use. Use either ointment for anti-inflammatory, antipruritic, antifungal, and antibacterial treatment of superficial bacterial infections, and for dermatologic disorders characterized by inflammation and dry or exudative dermatitis, particularly associated with bacterial or candidal (Candida albicans) infections.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

Topically: Use either ointment in dogs and cats for anti-inflammatory, antipruritic, antifungal, and antibacterial treatment of superficial bacterial infections, and for dermatologic disorders characterized by inflammation and dry or exudative dermatitis, particularly associated with bacterial or candidal (Candida albicans) infections.

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derma-Vet Cream

Treatment of the inflammation, edema, and secondary bacterial infections associated with topical ophthalmological conditions of the eye such as corneal injuries, incipient pannus, superficial keratitis, conjunctivitis, acute nongranulomatous anterior uveitis, kerato- conjunctivitis, and blepharitis.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Ophthalmic Solution

The drug is recommended for use in superficial ocular inflammations or infections limited to the conjunctiva or the anterior segment of the eye of cats, such as those associated with allergic reactions or gross irritants.

All topical ophthalmic preparations containing corticosteroids with or without an antimicrobial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until the infection is under control and corneal regeneration is well underway. For use only by or on the order of a licensed veterinarian.

Hydeltrone Ointment

A useful dressing for minor cuts, lacerations, abrasions, and post-surgical therapy in the cat. It may also be used following amputation of dewclaw, tails and claws, following ear trimming and castrating operations.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

It is indicated for treating acute otitis externa and, to a lesser degree, chronic otitis externa in cats. In treatment of ear canker and other inflammatory conditions of the external ear canal.

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® with Tetracaine

The drug is intended for use in cats for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycane Ophthalmic Ointment

For treating infections, allergic, and traumatic keratitis, conjunctivitis, acute otitis externa and, to a lesser degree, chronic otitis externa in cats.

All topical ophthalmic preparations containing corticosteroids, with or without an antimicrobial agent, are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non-susceptible organisms or to prolonged use on antibiotic-containing preparations resulting in overgrowth of non-susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® Sterile Ointment

The drug is indicated for treating infectious allergic and traumatic keratitis and conjunctivitis, otitis externa, and chronic otitis externa in cats.

All topical ophthalmic preparations containing corticosteroids with or without an anti-microbial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Delta Cortef® Sterile Solution

The drug is recommended for use as an aid in the treatment of bacterial, mycotic, and inflammatory dermatoses and otitis externa in cats.

For use only by or on order of a licensed veterinarian.

Tresaderm Dermatologic Solution

Treatment of superficial bacterial infections of the eyelid and conjunctiva of dogs and cats when due to susceptible organisms.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Vetropolycin Ophthalmic Ointment

Otitis and cysts: Use petrolatum base ointment in cats for the treatment of acute and chronic otitis and interdigital cysts.

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Panolog® Ointment

Administer to cats for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Neomycin is not for use parenterally in food-producing animals because of prolonged residues in edible tissues. Labeling shall bear an appropriate expiration date. For use by or on the order of a licensed veterinarian.

Biosol® Sterile Solution

For cystic areas. Use petrolatum base ointment for the treatment of interdigital cysts and for anal gland infections.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Animax® Ointment

For treating acute otitis externa and as adjunctive therapy in management of chronic otitis externa.

Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Liquisone F with Cerumene

For otic use. Use petrolatum base ointment for the treatment of acute and chronic otitis.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

For cystic areas. Use petrolatum base ointment for the treatment of interdigital cysts.

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian

Derm-Otic Ointment

Treating acute or chronic conjunctivitis caused by susceptible organisms.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Bacitracin-Neomycin-Polymyxin with Hydrocortisone Acetate Ophthalmic Ointment

It is used in the treatment of wound infections in cats.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-synalar Cream

Cattle (excluding veal calves)

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

Cattle (excluding veal calves)

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day before slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Sol® 50

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

Neomix® 325 Soluble Powder

Calves (Up to 250 Lbs)

For treatment of bacterial enteritis caused by E. coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Growing Cattle (Over 400 Lbs)

For reduction of liver condemnation due to liver abscesses.

Feed continuously. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Calves, Beef Cattle, and Non-Lactating Dairy

Calves and beef and non-lactating dairy cattle: For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

For the prevention and treatment of the early stages of shipping fever complex.

Feed 3-5 days before and after arrival in feedlots. A withdrawal period has not been established for use in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Neo-Oxy 100/100 MR®

Calves (up to 250 Lbs)

For treatment of bacterial enteritis caused by E. coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100D

Calves, Beef Cattle, and Non-Lactating Dairy Cattle

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100D

Growing cattle (over 400 lb)

For reduction of liver condemnation due to liver abscesses.

Feed continuously. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Calves, Beef Cattle, and Non-lactating Dairy Cattle

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Cattle (calves up to 250 lbs)

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Feed continuously for 7 to 14 days; in milk replacers or starter feed. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in pre-ruminating calves. Do not use in calves to be processed for veal.

Neo-Oxy 100/100 MR®

Growing cattle (over 400 lbs)

For the reduction of the incidence of liver abscesses.

Feed continuously.

Neo-Oxy 100/100 MR®

Cattle (calves and beef and nonlactating dairy cattle)

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Feed continuously for 7-14 days in feed or milk replacers. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

Treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7-14 days. 5-day withdrawal before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Feed continuously for 7 to 14 days; withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

Breeding Swine

For breeding swine for control and treatment of Leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline

Feed continuously for not more than 14 days. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Swine (breeding)

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira Pomona susceptible to oxytetracycline.

Feed continuously for not more than 14 days; withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

Breeding swine

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira Pomona susceptible to oxytetracycline.

Feed continuously for not more than 14 days; withdraw 5 days before slaughter.

Neo-Oxy 50/50®

Turkeys (growing)

For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days.

Neo-Sol® 50

Turkeys (growing)

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neosol-Oral

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not feed to turkeys producing eggs for human consumption. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Feed continuously for 7 to 14 days; withdraw 5 days before slaughter; do not feed to turkeys producing eggs for human consumption.

Neo-Oxy 100/100 MR®

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Feed continuously for 7 to 14 days; do not feed to turkeys producing eggs for human consumption.

Neo-Oxy 100/100 MR®

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Feed continuously for 7-14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. Withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7-14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin.

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Feed continuously for 7-14 days; do not feed to chickens producing eggs for human consumption; in low calcium feed, withdraw 3 days before slaughter.

Neo-Oxy 100/100 MR®

For control of infectious synovitis caused by Mycoplasma synoviae, control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Feed continuously for 7-14 days; do not feed to chickens producing eggs for human consumption; in low calcium feed, withdraw 3 days before slaughter.

Neo-Oxy 100/100 MR®

For reduction of mortality due to air sacculitis (air sac infection) caused by Escherichia coli susceptible to oxytetracycline.

Feed continuously for 5 days; do not feed to chickens producing eggs for human consumption; withdraw 24 hours before slaughter; in low calcium feed, withdraw 3 days before slaughter.

Neo-Oxy 100/100 MR®

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

Cattle, swine, sheep, and goats, and their offspring

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep, goats and their offspring.

Neomix Ag® 325

Dogs, cats, and horses

Indicated in the treatment or adjunctive therapy of certain ear and skin conditions in dogs, cats and horses caused by or associated with neomycin-susceptible organisms and/or allergy. In addition, it is indicated as superficial dressing applied to minor cuts, wounds, lacerations, abrasions, and for post-surgical application where reduction of pain and inflammatory response is deemed desirable. NEO-PREDEF with Tetracaine Powder may be used as a dusting powder following amputation of tails, claws, and dew-claws; following ear trimming and castrating; and following such surgical procedure as ovariohysterectomies. Applied superficially, it has been used successfully in the treatment of acute otitis externa in dogs, acute moist dermatitis and interdigital dermatitis in the dog, and as a dusting powder to various minor cuts, lacerations, and abrasions in the horse, cat and dog.

Neo-Predef® with Tetracaine Powder

A useful dressing for minor cuts, lacerations, abrasions, and post-surgical therapy in the horse. It may also be used following amputation of dewclaw, tails and claws, following ear trimming and castrating operations.

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

Indications For Use Use Level of Oxytetracycline and Neomycin Sulfate lbs. of Neo-Oxy 50/50® per ton of Type C Medicated Feed Chickens For control of infectious synovitis caused by Mycoplasma synoviae, control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline. Feed continuously for 7-14 days. 100-200g/ton 2.0-4.0 For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline. Feed continuously for 7-14 days. 400g/ton 8.0 For reduction of mortality due to air sacculitis (air sac infection) caused by Escherichia coli susceptible to oxytetracycline. Feed continuously for 5 days. 500g/ton 10.0 RESIDUE WARNING: AT 500 G/TON LEVEL, WITHDRAW 24 HOURS BEFORE SLAUGHTER. ZERO-DAY WITHDRAWAL PERIOD FOR LOWER USE LEVELS. IN LOW CALCIUM FEEDS WITHDRAW 3 DAYS BEFORE SLAUGHTER. DO NOT FEED TO CHICKENS PRODUCING EGGS FOR HUMAN CONSUMPTION. Turkeys For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline. Feed continuously for 7-14 days. 100g/ton 2.0 For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline. Feed continuously for 7-14 days. 200g/ton 4.0 For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline. Feed continuously for 7-14 days. 25 mg/lb body weight/day 16.7If bird weighs 10 lb, consuming 0.6 lb of complete feed per day RESIDUE WARNING: AT 200 G/TON USE LEVEL OR HIGHER, WITHDRAW 5 DAYS BEFORE SLAUGHTER. ZERO-DAY WITHDRAWAL PERIOD AT 100G/TON USE LEVELS. DO NOT FEED TO TURKEYS PRODUCING EGGS FOR HUMAN CONSUMPTION. Sheep For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Feed continuously for 7-14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 10 mg/lb body weight/day 24If lamb weighs 60 lb, consuming 1 lb of supplement per head per day RESIDUE WARNING: WITHDRAW 5 DAYS BEFORE SLAUGHTER AT 10 MG/LB DOSAGE. Swine For Swine: For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Feed continuously for 7-14 days. 10 mg/lb body weight/day 10If pig weighs 100 lb, consuming 4 lb of complete feed per day For Breeding Swine: For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline. Feed continuously for not more than 14 days. 10 mg/lb body weight/day 10 RESIDUE WARNING: WITHDRAW 5 DAYS BEFORE SLAUGHTER AT 10 MG/LB DOSAGE. Calves, Beef Cattle, and Nonlactating Dairy Cattle For Calves (up to 250 lbs.): For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Feed continuously for 7 to 14 days in starter feed. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 10 mg/lb body weight/day 20If calf weighs 100 lb, consuming 2 lb of complete starter feed per day For Growing Cattle (over 400 lbs.): For the reduction of the incidence of liver abscesses. Feed continuously. 75mg/head/day 1.5Include in feed supplement based on consumption of 2 lb of supplement per head per day For prevention and treatment of the early stages of shipping fever complex. Feed 3-5 days before and after arrival in feedlots. 0.5-2.0g/head/day 10-40 For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Feed continuously for 7-14 days in feed. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 10 mg/lb body weight/day 100If animal weighs 500 lb, consuming 2 lb of supplement per head per day RESIDUE WARNING: AT 0.5-2.0 G/HEAD/DAY AND 10 MG/LB DOSAGES: A WITHDRAWAL PERIOD HAS NOT BEEN ESTABLISHED FOR USE IN PRE-RUMINATING CALVES. DO NOT USE IN CALVES TO BE PROCESSED FOR VEAL. AT 0.5-2.0 G/HEAD/DAY AND 10 MG/LB DOSAGES: A MILK DISCARD TIME HAS NOT BEEN ESTABLISHED FOR USE IN LACTATING DAIRY CATTLE. DO NOT USE IN FEMALE DAIRY CATTLE 20 MONTHS OF AGE OR OLDER. AT 10 MG/LB DOSAGE, WITHDRAW 5 DAYS BEFORE SLAUGHTER. USE OF MORE THAN ONE PRODUCT CONTAINING NEOMYCIN OR FAILURE TO FOLLOW WITHDRAWAL TIMES MAY RESULT IN ILLEGAL DRUG RESIDUES. Store at or below 25°C (77°F) with excursions permitted to 37°C (98.6°F) Approved by FDA under NADA # 138-939

Neo-Oxy 50/50®

Mixing and Use Directions Mix Neo-Oxy 100/100 MR® with non-medicated milk replacer to provide the following concentrations: INDICATIONS FOR USE Use Level of Oxytetracycline and Neomycin lbs. of Neo-Oxy 100/100 MR per ton of Type C Medicated Feed Mixing directions are for example only and are based on mixing 1 lb of dry milk replacer with 1 gallon of water. Calves (milk replacer) For Calves (up to 250 lb): For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible by neomycin. Feed continuously for 7-14 days in milk replacer or starter feed. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 10 mg/lb body weight/day 20If calf weighs 100 lb, consuming 1 gallon of milk replacer per day. RESIDUE WARNING: A WITHDRAWAL PERIOD HAS NOT BEEN ESTABLISHED FOR USE IN PRERUMINATING CALVES. DO NOT USE IN CALVES TO BE PROCESSED FOR VEAL. A MILK DISCARD TIME HAS NOT BEEN ESTABLISHED FOR USE IN LACTATING DAIRY CATTLE. DO NOT USE IN FEMALE DAIRY CATTLE 20 MONTHS OR OLDER, INCLUDING DRY DAIRY COWS. USE IN THESE CATTLE MAY CAUSE DRUG RESIDUES IN MILK AND/OR IN CALVES BORN TO THESE COWS. WITHDRAW 5 DAYS BEFORE SLAUGHTER. USE OF MORE THAN ONE PRODUCT CONTAINING NEOMYCIN OR FAILURE TO FOLLOW WITHDRAWAL TIMES MAY RESULT IN ILLEGAL DRUG RESIDUES Calves, Beef Cattle, and Nonlactating Dairy Cattle For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible by neomycin. Feed continuously for 7-14 days in feed or milk replacers. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 10 mg/lb body weight/day 20 RESIDUE WARNINGS: A WITHDRAWAL PERIOD HAS NOT BEEN ESTABLISHED FOR USE IN PRERUMINATING CALVES. DO NOT USE IN CALVES TO BE PROCESSED FOR VEAL. A MILK DISCARD TIME HAS NOT BEEN ESTABLISHED FOR USE IN LACTATING DAIRY CATTLE. DO NOT USE IN FEMALE DAIRY CATTLE 20 MONTHS OR OLDER, INCLUDING DRY DAIRY COWS. USE IN THESE CATTLE MAY CAUSE DRUG RESIDUES IN MILK AND/OR IN CALVES BORN TO THESE COWS. WITHDRAW 5 DAYS BEFORE SLAUGHTER. USE OF MORE THAN ONE PRODUCT CONTAINING NEOMYCIN OR FAILURE TO FOLLOW WITHDRAWAL TIMES MAY RESULT IN ILLEGAL DRUG RESIDUES Store at or below 25°C (77°F) with excursions permitted to 37°C (98.6°F). Approved by FDA under NADA # 138-939

Neo-Oxy 100/100 MR®

Dermatologic Solution TRESADERM is indicated as an aid in the treatment of certain bacterial, mycotic, and inflammatory dermatoses and otitis externa in dogs and cats. Both acute and chronic forms of these skin disorders respond to treatment with TRESADERM. Many forms of dermatosis are caused by bacteria (chiefly Staphylococcus aureus, Proteus vulgaris and Pseudomonas aeruginosa). Moreover, these organisms often act as opportunistic or concurrent pathogens that may complicate already established mycotic skin disorders, or otoacariasis caused by Otodectes cynotis. The principal etiologic agents of dermatomycoses in dogs and cats are species of the genera Microsporum and Trichophyton. The efficacy of neomycin as an antibacterial agent, with activity against both gram-negative and gram-positive pathogens, is well documented. Detailed studies in various laboratories have verified the significant activity thiabendazole displays against the important dermatophytes. Dexamethasone, a synthetic adrenocorticoid steroid, inhibits the reaction of connective tissue to injury and suppresses the classic inflammatory manifestations of skin disease. The formulation for TRESADERM combines these several activities in a complementary form for control of the discomfort and direct treatment of dermatitis and otitis externa produced by the above-mentioned infectious agents.

Tresaderm® (thiabendazole, dexamethasone, neomycin sulfate solution)

NEO-PREDEF with Tetracaine Powder is indicated in the treatment or adjunctive therapy of certain ear and skin conditions in dogs, cats and horses caused by or associated with neomycin-susceptible organisms and/or allergy. In addition, it is indicated as superficial dressing applied to minor cuts, wounds, lacerations, abrasions, and for post-surgical application where reduction of pain and inflammatory response is deemed desirable. NEO-PREDEF with Tetracaine Powder may be used as a dusting powder following amputation of tails, claws, and dew-claws; following ear trimming and castrating; and following such surgical procedure as ovariohysterectomies. Applied superficially, it has been used successfully in the treatment of acute otitis externa in dogs, acute moist dermatitis and interdigital dermatitis in the dog, and as a dusting powder to various minor cuts, lacerations, and abrasions in the horse, cat and dog.

Neo-Predef® with Tetracaine Powder

Antibacterial - Neomycin Sulfate Oral Solution for Cattle, Swine, Sheep and Goats For Animal Use Only Keep Out of Reach of Children CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Approved by FDA under ANADA # 200-379 INDICATIONS: Indicated for the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep and goats. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. If symptoms such as fever, depression, or going off feed develop, oral neomycin is not indicated as the sole treatment since systemic levels of neomycin are not obtained due to low absorption from the gastrointestinal tract.

Neovet

Neomycin Sulfate Antibacterial FOR ANIMAL USE ONLY KEEP OUT OF REACH OF CHILDREN Indicated for the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep and goats. Contains per mL: neomycin sulfate 200 mg equivalent to 140 mg neomycin CAUTION: Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Restricted Drug-Use Only As Directed (California) For Oral Use in Animals only. Indicated for the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep and goats. ANADA#: 200-379 Approved by F.D.A.

NEOMYCIN LIQUID

Animax Ointment is particularly useful in the treatment of acute and chronic otitis of varied etiologies, in interdigital cysts in cats and dogs and in anal gland infections in dogs. The preparation is also indicated in the management of dermatologic disorders characterized by inflammation and dry or exudative dermatitis, particularly those caused, complicated, or threatened by bacterial or candidal (Candida albicans) infections. It is also of value in eczematous dermatitis, contact dermatitis, and seborrheic dermatitis; and as an adjunct in the treatment of dermatitis due to parasitic infestation.

Animax® Ointment (nystatin-neomycin sulfate-thiostrepton-triamcinolone acetonide ointment)

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves), swine, sheep and goats. For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys. Huvepharma® Manufactured for: Huvepharma, Inc. 525 Westpark Dr., Suite 230 Peachtree City, GA 30269 Each Packet Contains: 1430 gm neomycin sulfate equivalent to 1000 gm neomycin.

FDA application 200-130

Antibacterial Not For Use in Humans Keep Out of Reach of Children Restricted Drug - Use Only as Directed (California) For Oral Use in Animals Only Approved by FDA under ANADA # 200-379 CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Indicated for the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep and goats.

Neomycin (Neomycin Sulfate)

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves), swine, sheep and goats. For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys. Each Pound Contains: 325 g neomycin sulfate equivalent to 227.5 g neomycin.

FDA application 200-130

NeoPlex™ is a broad spectrum antibiotic effective against most external infections of both marine and freshwater fish. Used as directed, NeoPlex™ will not discolor the water or damage the filter bed. It is well tolerated by invertebrates, although delicate species may be stressed.

Neoplex™

For the treatment of superficial bacterial infections of the eyelid and conjunctiva of dogs and cats when due to organisms susceptible to one or more of the antibiotics contained in the ointment

Federal law restricts this drug to use by or on the order of a licensed veterinarian

Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment

FOR USE IN ANIMAL FEEDS ONLY NOT FOR HUMAN USE RESTRICTED DRUG (CALIFORNIA) – USE ONLY AS DIRECTED

Neo-Terramycin® 100/100 (neomycin-oxytetracycline) TYPE A MEDICATED ARTICLE

As an aid in the treatment of bacterial, mycotic, and inflammatory dermatoses and otitis externa

Federal law restricts this drug to use by or on the order of a licensed veterinarian

Thiabendazole, Dexamethasone, Neomycin Sulfate Solution

FOR USE IN THE MANUFACTURE OF MEDICATED ANIMAL FEEDS

Neo-Oxy 50/50®

Before instilling any medication into the ear, examine the external ear canal thoroughly to be certain the tympanic membrane is not ruptured in order to avoid the possibility of transmitting infection to the middle ear as well as damaging the cochlea or vestibular apparatus from prolonged contact. If hearing or vestibular dysfunction is noted during the course of treatment, discontinue the use of Animax Ointment.

Animax® Ointment (nystatin-neomycin sulfate-thiostrepton-triamcinolone acetonide ointment)

Residue Warnings: Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species: Cattle 1 day Swine and Goats 3 days Sheep 2 days Turkeys 0 days A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. The Safety Data Sheet (SDS) contains more detailed occupational safety information. To report suspected adverse drug events, for technical assistance or to obtain a copy of the SDS, contact Bimeda, Inc. at 1-888-524-6332. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at www.fda.gov/reportanimalae.

FDA application 200-050

Caution: To administer the stated dosage, the concentration of neomycin required in medicated water must be adjusted to compensate for variation in age and weight of animal, the nature and severity of disease signs, and environmental temperature and humidity, each of which affects water consumption. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. If symptoms such as fever, depression, or going off feed develop, oral neomycin is not indicated as the sole treatment since systemic levels of neomycin are not obtained due to low absorption from the gastrointestinal tract. Important: Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days for cattle, swine, sheep and goats and 5 days for turkeys. Animals not drinking or eating should be treated individually by drench. Warning: Not for human use. Keep out of reach of children.

FDA application 200-050

CAUTION: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian. CAUTION: For use in manufacturing medicated animal feeds only. CAUTION: Certain components of animal feeds, including medicated premixes, possess properties that may be a potential health hazard or a source of personal discomfort to certain individuals who are exposed to them. Human exposure should, therefore, be minimized by observing the general industry standards for occupational health and safety. Precautions such as the following should be considered: dust masks or respirators and protective clothing should be worn; dust-arresting equipment and adequate ventilation should be utilized; personal hygiene should be observed; wash before eating or leaving a work site; be alert for signs of allergic reactions—seek prompt medical treatment if such reactions are suspected.

Neo-Terramycin® 100/100 (neomycin-oxytetracycline) TYPE A MEDICATED ARTICLE

Warning: Not for human use. Keep out of reach of children. Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species. Cattle...............................................................................1 day Swine and goats ............................................................3 days Sheep.............................................................................2 days A withdrawal period has not been established for this product in pre-rumination calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

NEOSOL™ Soluable Powder

Not for human use. Keep out of reach of children. Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species: Cattle .............................................. 1 day Sheep ............................................ 2 days Swine and Goats ............................. 3 days Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

NEOMYCIN LIQUID

Not for human use. Keep out of reach of children. Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species: Cattle 1 day Sheep 2 days Swine and Goats 3 days A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months or age or older. Use of more than one product containing neomycin or failure to sollow withdrawal times may result in illegal drug residues. RESTRICTED DRUG-USE ONLY AS DIRECTED (CALIFORNIA) FOR ORAL USE IN ANIMALS ONLY.

Neovet

Residue Warnings: Discontinue treatment prior to slaughter by at least the number of days listed below for the appropriate species: Turkeys ...................... 0 days Cattle ........................ 1 day Sheep ........................ 2 days Swine and goats ......... 3 days A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

FDA application 200-130

Not for human use. Do not use in horses intended for human consumption. Clinical and experimental data have demonstrated that corticosteroids administered orally or by injection to animals may induce the first stage of parturition if used during the last trimester of pregnancy and may precipitate premature parturition followed by dystocia, fetal death, retained placenta and metritis. Additionally, corticosteroids administered to dogs, rabbits, and rodents during pregnancy have resulted in cleft palate in offspring. Corticosteroids administered to dogs during pregnancy have also resulted in other congenital anomalies, including deformed forelegs, phocomelia, and anasarca.

Neo-Predef® with Tetracaine Powder

Not for human use. Keep out of reach of children. Discontinue treatment prior to slaughter by at least the number of days listed below for appropriate species: Cattle ....................... 1 day Sheep ...................... 2 days Swine and Goats ....... 3 days A withdrawal period has not been established for this product in pre-ruminating calves. Do no use in claves to be processed for veal. A milk discard period has not been established for this product in lactating dairy cattle. Do no use in female dairy cattle 20 months of age or older. Use of more than one product containing Neomycin or failure to follow withdrawal times may result in illegal drug residues.

Neomycin (Neomycin Sulfate)

Clinical and experimental data have demonstrated that corticosteroids administered orally or by injection to animals may induce the first stage of parturition if used during the last trimester of pregnancy and may precipitate premature parturition followed by dystocia, fetal death, retained placenta, and metritis. Additionally, corticosteroids administered to dogs, rabbits and rodents during pregnancy have resulted in cleft palate in the offspring. In dogs, other congenital anomalies have resulted: deformed forelegs, phocomelia, and anasarca. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Animax® Ointment (nystatin-neomycin sulfate-thiostrepton-triamcinolone acetonide ointment)

For topical use in dogs and cats. Avoid contact with eyes. Keep this and all drugs out of the reach of children. The Safety Data Sheet (SDS) contains more detailed occupational safety information. To report suspected adverse drug events, for technical assistance, or to obtain a copy of the Safety Data Sheet (SDS), contact Boehringer Ingelheim Animal Health USA Inc. at 1-888-637-4251. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or online at www.fda.gov/reportanimalae.

Tresaderm® (thiabendazole, dexamethasone, neomycin sulfate solution)

For use in ornamental aquariums only. Not for human consumption.

Neoplex™

SAP and SGPT (ALT) enzyme elevations, polydipsia and polyuria, vomiting, and diarrhea (occasionally bloody) have been observed following parenteral or systemic use of synthetic corticosteroids in dogs. Cushing's syndrome has been reported in association with prolonged or repeated steroid therapy in dogs. Temporary hearing loss has been reported in conjunction with treatment of otitis with products containing corticosteroids. However, regression usually occurred following withdrawal of the drug. Hearing loss, with varying degrees of recovery, has been reported with the use of Animax Ointment. If hearing dysfunction is noted during the course of treatment with Animax Ointment, discontinue its use. To report suspected adverse drug events, for technical assistance or to obtain a copy of the safety data sheet (SDS), contact Dechra at (866) 933-2472. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at http://www.fda.gov/reportanimalae.

Animax® Ointment (nystatin-neomycin sulfate-thiostrepton-triamcinolone acetonide ointment)

Contact Information: To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Huvepharma, Inc. at 1-877-994-4883 or www.huvepharma.us. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae

FDA application 200-130

In treatment of otitis externa and other inflammatory conditions of the external ear canal a quantity of ointment sufficient to fill the external ear canal may be applied one to three times daily. When used on the skin or mucous membranes, the affected area should be cleansed, and a small amount of the ointment applied and spread or rubbed in gently. The involved area may be treated one to three times a day and these daily applications continued in accordance with the clinical response.

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

Clean ear canal of impacted cerumen, remove any foreign bodies such as grass awns and ticks, and instill three to five drops of petrolatum base ointment. Preliminary use of a local anesthetic may be advisable. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

A small quantity of the ointment should be expressed into the conjunctival sac 4 times a day (at intervals of 1 to 8 hours) for a few days until there is a favorable response, then the frequency of application may be reduced to twice daily as long as the condition remains under control. Treatment may require from a few days to several weeks.

Ophthalmic, Topical

All topical ophthalmic preparations containing corticosteroids with or without an antimicrobial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until the infection is under control and corneal regeneration is well underway. For use only by or on the order of a licensed veterinarian.

Hydeltrone Ointment

For otic use: Clean ear canal of impacted cerumen, remove any foreign bodies such as grass awns and ticks, and instill three to five drops of petrolatum base ointment. Preliminary use of a local anesthetic may be advisable. For infected anal glands and cystic areas: Drain gland or cyst and fill with petrolatum base ointment.

Topical

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Panolog® Ointment

In treating dermatoses affecting areas other than the ear, the surface of the lesions should be well moistened (two to four drops per square inch) twice daily. In treating otitis externa, five to 15 drops of the drug should be instilled in the ear twice daily. The is limited to 7 days maximum duration of administration.

Topical

For use only by or on order of a licensed veterinarian.

Tresaderm Dermatologic Solution

For beginning treatment of acute ocular inflammations 1 or 2 drops may be placed in the conjunctival sac 3 to 6 times during a 24 hour period. When improvement occurs, the dosage may be reduced to 1 drop 2 to 4 times daily. In otitis externa, 2 to 6 drops may be placed in the external ear canal 2 or 3 times daily.

Ophthalmic

All topical ophthalmic preparations containing corticosteroids with or without an anti-microbial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Delta Cortef® Sterile Solution

Clean affected areas and remove any encrusted discharge or exudate, and apply sparingly either ointment in a thin film. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

Apply three or four times daily into the conjunctival sac. With improvement, frequency may be reduced to two or three times daily. For treatment of ear canker and other inflammatory conditions of the external ear canal, fill external ear canal one to three times daily.

Ophthalmic

All topical ophthalmic preparations containing corticosteroids, with or without an antimicrobial agent, are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non-susceptible organisms or to prolonged use on antibiotic-containing preparations resulting in overgrowth of non-susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® Sterile Ointment

For mild inflammations, application may range from once daily to once a week; for severe conditions Animax Ointment may be applied as often as two to three times daily, if necessary. Frequency of treatment may be decreased as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Animax® Ointment

Drain gland or cyst and fill with petrolatum base ointment. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

10 to 20 pounds body weight- 1 capsule orally twice daily to dogs. 20 to 30 pounds body weight- 2 capsules orally twice daily to dogs. Over 30 pounds body weight- 3 capsules orally twice daily to dogs.

Oral

Do not continue medication longer than 5 days. Overdosage or prolonged administration may produce nephrotoxicity as manifested by albuminuria, presence of granular casts and depressed urinary output. If it is desirable to administer a vasoconstrictor, norepinephrine is the drug of choice. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Darbazine Spansule Capsule No.1

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Intramuscular, Intravenous

Neomycin is not for use parenterally in food-producing animals because of prolonged residues in edible tissues. Labeling shall bear an appropriate expiration date. For use by or on the order of a licensed veterinarian.

Biosol® Sterile Solution

For topical dermatological use: Clean affected areas and remove any encrusted discharge or exudate, and apply sparingly either ointment in a thin film.

Topical

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derma-Vet Cream

Rub a small amount into the involved area 1 to 3 times a day. After definite improvement, it may be applied once a day or every other day.

Topical

For use in dogs only. Shake drug thoroughly and clean lesion before using. If redness, irritation, or swelling persists or increases, discontinue use and reevaluate diagnosis. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Forte Topical® Ointment

Over 30 pounds body weight- 1 capsule orally twice daily to dogs. Over 60 pounds- 2 capsules orally twice daily to dogs.

Oral

Do not continue medication longer than 5 days. Overdosage or prolonged administration may produce nephrotoxicity as manifested by albuminuria, presence of granular casts and depressed urinary output. If it is desirable to administer a vasoconstrictor, norepinephrine is the drug of choice. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Darbazine Spansule Capsule No.3

It is administered at a dosage level of one to two tablets per 10 pounds of body weight twice daily for 3 days.

Oral

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Jenomycin Tablets

A quantity of ointment sufficient to fill the external ear canal may be applied one to three times daily.

Topical

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® with Tetracaine

A small amount is applied to the infected area two or three times daily.

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-synalar Cream

Apply a thin film over the cornea three or four times daily.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Bacitracin-Neomycin-Polymyxin with Hydrocortisone Acetate Ophthalmic Ointment

Instill 1 to 2 drops per eye every 6 hours.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Opthakote Ophthalmic

Apply 2 to 3 drops per eye, every 4 hours.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Ophthalmic Solution

The drug is applied four times each day.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycane Ophthalmic Ointment

2 to 3 applications daily or as needed.

Topical

Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Liquisone F with Cerumene

Clean ear canal of impacted cerumen, remove any foreign bodies such as grass awns and ticks, and instill three to five drops of petrolatum base ointment. Preliminary use of a local anesthetic may be advisable. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

A small quantity of the ointment should be expressed into the conjunctival sac 4 times a day (at intervals of 1 to 8 hours) for a few days until there is a favorable response, then the frequency of application may be reduced to twice daily as long as the condition remains under control. Treatment may require from a few days to several weeks.

Ophthalmic, Topical

All topical ophthalmic preparations containing corticosteroids with or without an antimicrobial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until the infection is under control and corneal regeneration is well underway. For use only by or on the order of a licensed veterinarian.

Hydeltrone Ointment

In treating dermatoses affecting areas other than the ear, the surface of the lesions should be well moistened (two to four drops per square inch) twice daily. In treating otitis externa, five to 15 drops of the drug should be instilled in the ear twice daily. The is limited to 7 days maximum duration of administration.

Topical

For use only by or on order of a licensed veterinarian.

Tresaderm Dermatologic Solution

For beginning treatment of acute ocular inflammations 1 or 2 drops may be placed in the conjunctival sac 3 to 6 times during a 24 hour period. When improvement occurs, the dosage may be reduced to 1 drop 2 to 4 times daily. In otitis externa, 2 to 6 drops may be placed in the external ear canal 2 or 3 times daily.

Ophthalmic

All topical ophthalmic preparations containing corticosteroids with or without an anti-microbial agent are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Delta Cortef® Sterile Solution

For otic use: Clean ear canal of impacted cerumen, remove any foreign bodies such as grass awns and ticks, and instill three to five drops of petrolatum base ointment. Preliminary use of a local anesthetic may be advisable. For cystic areas: Drain gland or cyst and fill with petrolatum base ointment.

Topical

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Panolog® Ointment

When used on the skin or mucous membranes, the affected area should be cleansed, and a small amount of the ointment applied and spread or rubbed in gently. The involved area may be treated one to three times a day and these daily applications continued in accordance with the clinical response.

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

Clean affected areas and remove any encrusted discharge or exudate, and apply sparingly either ointment in a thin film. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derm-Otic Ointment

Apply three or four times daily into the conjunctival sac. With improvement, frequency may be reduced to two or three times daily. For treatment of ear canker and other inflammatory conditions of the external ear canal, fill external ear canal one to three times daily.

Ophthalmic

All topical ophthalmic preparations containing corticosteroids, with or without an antimicrobial agent, are contraindicated in the initial treatment of corneal ulcers. They should not be used until infection is under control and corneal regeneration is well underway. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non-susceptible organisms or to prolonged use on antibiotic-containing preparations resulting in overgrowth of non-susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® Sterile Ointment

For mild inflammations, application may range from once daily to once a week; for severe conditions Animax Ointment may be applied as often as two to three times daily, if necessary. Frequency of treatment may be decreased as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Animax® Ointment

Drain gland or cyst and fill with petrolatum base ointment. For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs.

Topical

Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

DERMA-VET® Ointment

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Intramuscular, Intravenous

Neomycin is not for use parenterally in food-producing animals because of prolonged residues in edible tissues. Labeling shall bear an appropriate expiration date. For use by or on the order of a licensed veterinarian.

Biosol® Sterile Solution

For topical dermatological use: Clean affected areas and remove any encrusted discharge or exudate, and apply sparingly either ointment in a thin film.

Topical

For mild inflammations, use once daily to once a week. For severe conditions, apply initially two to three times daily, decreasing frequency as improvement occurs. Not intended for treatment of deep abscesses or deep-seated infections. Not for ophthalmic use. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Derma-Vet Cream

A quantity of ointment sufficient to fill the external ear canal may be applied one to three times daily.

Topical

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Cortef® with Tetracaine

A small amount is applied to the infected area two or three times daily.

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-synalar Cream

Apply a thin film over the cornea three or four times daily.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Bacitracin-Neomycin-Polymyxin with Hydrocortisone Acetate Ophthalmic Ointment

Apply 2 to 3 drops per eye, every 4 hours.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Anaprime® Ophthalmic Solution

The drug is applied four times each day.

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycane Ophthalmic Ointment

2 to 3 applications daily or as needed.

Topical

Tetracaine and neomycin have the potential to sensitize. If signs of irritation or sensitivity develop, discontinue use. Prolonged use of this product may result in overgrowth of non-susceptible organisms. If new infections due to bacteria or fungi appear during therapy, appropriate measures should be taken. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Liquisone F with Cerumene

Cattle (excluding veal calves)

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Oral

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle (not for use in veal calves). Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neosol-Oral

Cattle (excluding veal calves)

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Oral

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Biosol® Liquid

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Oral

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Sulfate

Calves (Up to 250 Lbs)

10 mg/lb of body weight daily

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Calves (Up to 250 Lbs)

10 mg/lb BW

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Growing Cattle (Over 400 Lbs)

75 mg/head/day

Oral

Feed continuously. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Calves, Beef Cattle, and Non-Lactating Dairy

10 mg/lb body weight (BW)

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

0.5 to 2.0 g/head/day

Oral

Feed 3 to 5 days before and after arrival in feedlots. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Calves (up to 250 Lbs)

In Milk Replacer: 10 mg/lb of body weight daily

Oral

Feed continuously for 7-14 days If symptoms persist after using for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms.

Neo-Terramycin® 50/50D

Calves (up to 250 Lbs)

10 mg/lb of body weight daily

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100D

Calves, Beef Cattle, and Non-Lactating Dairy Cattle

10 mg/lb of body weight daily

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50D

Calves, Beef Cattle, and Non-Lactating Dairy Cattle

10 mg/lb of body weight

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100D

Growing cattle (over 400 lb)

75 mg/head/day

Oral

Feed continuously. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Calves, Beef Cattle, and Non-lactating Dairy Cattle

10 mg/lb of body weight daily

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Cattle (calves up to 250 lbs)

10 mg/lb body weight/day

Oral

Feed continuously for 7 to 14 days; in milk replacers or starter feed. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in pre-ruminating calves. Do not use in calves to be processed for veal.

Neo-Oxy 100/100 MR®

Growing cattle (over 400 lbs)

75 mg/head/day

Oral

Feed continuously.

Neo-Oxy 100/100 MR®

Cattle (calves and beef and nonlactating dairy cattle)

10 mg/lb body weight/day

Oral

Feed continuously for 7-14 days in feed or milk replacers. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. A withdrawal period has not been established for use in pre-ruminating calves. Do not use in calves to be processed for veal. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. Withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Oral

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Oral

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Biosol® Liquid

10 mg/lb of body weight daily.

Oral

Feed continuously for 7-14 days. 5-day withdrawal before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

10 mg/lb BW

Oral

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Breeding Swine

10 mg/lb of body weight daily

Oral

Feed continuously for not more than 14 days. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Breeding Swine

10 mg/lb BW

Oral

Feed continuously for not more than 14 days. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

Swine (breeding)

10 mg/lb/body weight/day

Oral

Feed continuously for not more than 14 days; withdraw 5 days before slaughter.

Neo-Oxy 100/100 MR®

Breeding swine

10 mg/lb/body weight/day

Oral

Feed continuously for not more than 14 days; withdraw 5 days before slaughter.

Neo-Oxy 50/50®

Turkeys (growing)

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Oral

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days.

Neo-Sol® 50

25 mg/lb of body weight daily

Oral

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not feed to turkeys producing eggs for human consumption. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

25 mg/lb BW

Oral

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not feed to turkeys producing eggs for human consumption. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

100 g/ton

Oral

Feed continuously for 7 to 14 days. Do not feed to turkeys producing eggs for human consumption. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

200 g/ton

Oral

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not feed to turkeys producing eggs for human consumption. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Oral

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Oral

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Biosol® Liquid

10 mg/lb of body weight daily

Oral

Feed continuously for 7-14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

10 mg/lb of body weight

Oral

Feed continuously for 7 to 14 days. Treatment should continue 24 to 48 hours beyond remission of disease symptoms. Withdraw 5 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

100 to 200 g/ton

Oral

Feed continuously for 7-14 days; do not feed to chickens producing eggs for human consumption; in low calcium feed, withdraw 3 days before slaughter.

Neo-Oxy 100/100 MR®

100-200 g/ton.

Oral

Feed continuously for 7-14 days. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

500 g/ton.

Oral

Feed continuously for 5 days. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 50/50

400 g/ton

Oral

Feed continuously for 7 to 14 days. Do not feed to chickens producing eggs for human consumption. In low calcium feed, withdraw 3 days before slaughter. Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Neo-Terramycin® 100/100

Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Oral

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Oral Solution

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Oral

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Biosol® Liquid

Cattle, swine, sheep, and goats, and their offspring

Type C milk replacer 400 to 2,000 grams per ton. Type C feed 250 to 2,500 grams per ton.

Oral

Neomix Ag® 325

Dogs, cats, and horses

After cleaning the affected area, NEO-PREDEF with Tetracaine Powder is applied by compressing the sides of the container with short, sharp squeezes. In the most instances a single daily application will be sufficient; however, it may be applied one to three times daily, as required.

Topical

Neo-Predef® with Tetracaine Powder

When used on the skin or mucous membranes, the affected area should be cleansed, and a small amount of the ointment applied and spread or rubbed in gently. The involved area may be treated one to three times a day and these daily applications continued in accordance with the clinical response.

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Predef® with Tetracaine Top. Ointment

Thoroughly mix the amount of this Type A Medicated Article according to the directions below withat least an equal amount by weight of feed ingredients prior to blending into a complete feed. Indications for Use Oxytetracycline and Neomycin Amount lb. of Neo-Terramycin 100/100 per ton CHICKENS Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline 100-200 g/ton Feed continuously for 7-14 days 1-2 Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline 400 g/ton Feed continuously for 7-14 days 4 Reduction of mortality due to air sacculitis (air sac infection) caused by E. coli susceptible to oxytetracycline 500 g/ton Feed continuously for 5 days 5 WARNING: At 500 g/ton level, withdraw 24 hours before slaughter. Low calcium feeds at 500 g/ton, withdraw 3 days before slaughter. Zero-day withdrawal period for lower use levels. In low calcium feeds withdraw 3 days before slaughter. Do not administer to chickens producing eggs for human consumption. TURKEYS Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline 100 g/ton Feed continuously for 7-14 days 1 Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline 200 g/ton Feed continuously for 7-14 days 2 Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline 25 mg/lb of body weight daily Feed continuously for 7-14 days 8.351 WARNING: At 200 g/ton use level or higher, withdraw 5 days before slaughter. Zero-day withdrawal period for lower use levels. Do not administer to turkeys producing eggs for human consumption. SWINE Treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days 52 For breeding swine for control and treatment of Leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline 10 mg/lb of body weight daily Feed continuously for not more than 14 days 52 WARNING: 5-day withdrawal before slaughter at 10 mg/lb dosage. CALVES, BEEF CATTLE, AND NONLACTATING DAIRY CATTLE For growing cattle (over 400 lb) for reduction of liver condemnation due to liver abscesses 75 mg/head/day Feed continuously 0.753 Prevention and treatment of the early stages of shipping fever complex 0.5-2.0 g/head/day Feed 3-5 days before and after arrival in feedlots 5-203 Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 504 For calves (up to 250 lb) for treatment of bacterial enteritis caused by E. coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 105 WARNING: A withdrawal period has not been established in preruminating calves; do not use in calves to be processed for veal. At the 0.5-2.0 g/head/day and 10 mg/lb levels: A milk discard time has not been established for use in lactating dairy cattle; do not use in female dairy cattle 20 months of age or older. At the 10 mg/lb level, withdraw 5 days before slaughter. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. SHEEP Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 126 WARNING: 5-day withdrawal before slaughter at 10 mg/lb dosage. 1If bird weighs 10 lb, consuming 0.6 lb of complete feed per day 2If pig weighs 100 lb, consuming 4 lb of complete feed per day 3Include in feed supplement based on consumption of 2 lb of supplement per head per day 4If animal weighs 500 lb, consuming 2 lb of supplement per head per day 5If calf weighs 100 lb, consuming 2 lb of complete starter feed per day 6If lamb weighs 60 lb, consuming 1 lb of supplement per head per day

ORAL

Neo-Terramycin® 100/100 (neomycin-oxytetracycline) TYPE A MEDICATED ARTICLE

Add to drinking water - Not for use in liquid supplements. Dosage and Administration: Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Administer to turkeys at a dose of 10 mg neomycin sulfate per pound of body weight per day for 5 days. Using measuring spoons, the recommended dosage can be determined as follows: Daily Schedule For Drinking Water: SWINE One level tablespoon of NeoMed 325 added to water consumed in one day will treat Weight of each pig 50 pigs 10 pounds 20 pigs 25 pounds 10 pigs 50 pounds CATTLE One level tablespoon of NeoMed 325 added to water consumed in one day will treat Weight of each calf 10 calves 50 pounds 7 calves 75 pounds 4 calves 125 pounds TURKEYS One level tablespoon of NeoMed 325 added to water consumed in one day will treat Weight of each bird 1000 birds 0.5 pounds 500 birds 1 pounds 100 birds 5 pounds 50 birds 10 pounds The product should be added to the amount of drinking water estimated to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. For a stock solution, add six level tablespoons to one gallon of water. Each pint of this stock solution will medicate 5 gallons of drinking water. For use in Automatic Proportioners delivering 2 ounces of stock solution per gallon of drinking water, dissolve 9 level tablespoons in a gallon of water to make the stock solution. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds of body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12-24 hours.

ORAL

FDA application 200-050

Administer to cattle, swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight in divided doses for a maximum of 14 days. Dosage Schedule for treatment of colibacillosis: Pounds of Amount of Neomycin Liquid  Body Weight Per Day in Divided Doses 25 lbs. 1/4 teaspoonful 50 lbs. 1/2 teaspoonful 100 lbs 1 teaspoonful 300 lbs 1 tablespoonful 600 lbs 1 fluid ounce Teaspoon = U.S. Standard Measure Neomycin Liquid may be given undiluted or diluted with water. Herd Treatment: Each bottle will treat 9,600 pounds body weight. Therefore, estimate the total number of pounds body weight of the animals to be treated and administer one (1) fluid ounce for each 600 pounds. The product should be added to the amount of drinking water to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one(1) teaspoon in water or milk for each 100 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12-24 hours. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. If symptoms such as fever, depression, or going off feed develop, oral neomycin is not indicated as the sole treatment since systemic levels of neomycin are not obtained due to low absorption from the gastrointestinal tract. Important: Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Animals not drinking or eating should be treated individually by drench.

ORAL

Neomycin (Neomycin Sulfate)

Restricted Drug - Use only as Directed (California) For Oral Use in Animals Only Add to drinking water - Not for use in liquid supplements. Dosage and Administration: Administer 10 mg neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Using measuring spoons, the recommended dosage can be determined as follows: Daily Schedule for Drinking Water SWINE One tablespoonful* of Neosol Solubel Powder added to water consumed in one day will treat Weight of each pig 50 pigs 10 pounds 20 pigs 25 pounds 10 pigs 50 pounds CATTLE (Not to be used in veal calves) One tablespoonful* of Neosol Solubel Powder added to water or milk consumed in one day will treat Weight of calf 10 calves 50 pounds 7 calves 75 pounds 4 calves 125 pounds * Level Tablespoonful = US Standard Measure The product should be added to the amount of drinking water estimated to be consumed in 12 - 24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. For a stock solution, add six level tablespoonfuls to one gallon of water. Each pint of this stock solution will medicate 5 gallons of drinking water. For use in Automatic Proportioners delivering 2 ounces of stock solution per gallon of drinking water, dissolve 9 level tablespoonfuls in a gallon of water to make the stock solution. Individual Animal Treatment - To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds of body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12 – 24 hours.

ORAL

NEOSOL™ Soluable Powder

Mix Neo-Terramycin 100/100D with nonmedicated milk replacer to provide the following drug concentrations: Indications for Use Oxytetracycline and Neomycin Amount lb. of Neo-Terramycin 100/100D per ton1 CALVES (milk replacer) For calves (up to 250 lb) for treatment of bacterial enteritis caused by E. coli susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 202 CALVES, BEEF CATTLE, AND NONLACTATING DAIRY CATTLE Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline; treatment and control of colibacillosis (bacterial enteritis) caused by E. coli susceptible to neomycin 10 mg/lb of body weight daily Feed continuously for 7-14 days Treatment should continue 24 to 48 hours beyond remission of disease symptoms. 202 WARNING: A withdrawal period has not been established in preruminating calves; do not use in calves to be processed for veal. At the 10 mg/lb level, withdraw 5 days before slaughter. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. A milk discard time has not been established for use in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older. 1Mixing directions are for example only and are based on mixing 1 lb of dry milk replacer with 1 gallon of water. 2If calf weighs 100 lb, consuming 1 gallon of milk replacer per day.

ORAL

Neo-Terramycin® 100/100D (neomycin-oxytetracycline) TYPE A MEDICATED ARTICLE

Add to drinking water - Not for use in liquid supplements Dosage and Administration: Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Administer to turkeys at a dose of 10 mg neomycin sulfate per pound of body weight per day for 5 days. Herd/Flock Treatment: Each packet will treat 35,750 pounds body weight. Therefore, estimate the total number of pounds of body weight of the animals to be treated and administer one (1) packet (or portion thereof) for each 35,750 pounds. The product should be added to the amount of drinking water estimated to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12 - 24 hours. Drinking Water: Swine - Use the number of packets indicated below in 1,280 gallons of water, or in 10 gallons of stock solution used in proportioner set to meter one ounce per gallon. Pigs weighing 25 to 50 lbs..... 2 packets Pigs weighing 50 to 100 lbs... 3 packets Pigs weighing over 100 lbs.... 4 packets

ORAL

FDA application 200-130

Add to drinking water - Not for use in liquid supplements. Dosage and Administration: Administer to turkeys at a dose of 10 mg neomycin sulfate per pound of body weight per day for 5 days. Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Herd/Flock Treatment: Each packet will treat 7,150 pounds body weight. Therefore, estimate the total number of pounds of body weight of the animals to be treated and administer one (1) packet (or portion thereof) for each 7,150 pounds. The product should be added to the amount of drinking water estimated to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12 - 24 hours. Drinking Water: Swine - Use the number of packets indicated below in 256 gallons of water, or in two gallons of stock solution used in proportioner set to meter one ounce per gallon. Pigs weighing 25 to 50 lbs..... 2 packets Pigs weighing 50 to 100 lbs... 3 packets Pigs weighing over 100 lbs.... 4 packets

ORAL

FDA application 200-130

Add to drinking water - Not for use in liquid supplements. DOSAGE AND ADMINISTRATION: Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Administer to turkeys at a dose of 10 mg neomycin sulfate per pound of body weight per day for 5 days. Herd/Flock Treatment: Each packet will treat 7,150 pounds body weight. Therefore, estimate the total number of pounds of body weight of the animals to be treated and administer one (1) packet (or portion thereof) for each 7,150 pounds. The product should be added to the amount of drinking water estimated to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds of body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12-24 hours. Drinking Water: Swine Use the number of packets indicated below in 256 gallons of water, or in two gallons of stock solution used in proportioner set to meter one ounce per gallon. Pigs Weighing 25 to 50 Pounds 2 Packets Pigs Weighing 50 to 100 Pounds 3 Packets Pigs Weighing Over 100 Pounds 4 Packets

ORAL

FDA application 200-050

Add to drinking water - Not for use in liquid supplements. Dosage and Administration: Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Administer to turkeys at a dose of 10 mg neomycin sulfate per pound of body weight per day for 5 days. Herd/Flock Treatment: Each packet will treat 143,000 pounds body weight. Therefore, estimate the total number of pounds of body weight of the animals to be treated and administer one (1) packet (or portion thereof) for each 143,000 pounds. The product should be added to the amount of drinking water estimated to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) level teaspoon in water or milk for each 160 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12 - 24 hours. Drinking Water: Swine - Use the quantity indicated below in 5120 gallons of water, or in 40 gallons of stock solution used in proportioner set to meter one ounce per gallon. Pigs weighing 25 to 50 lbs..... 2 packets Pigs weighing 50 to 100 lbs... 3 packets Pigs weighing over 100 lbs.... 4 packets

ORAL

FDA application 200-130

Administer to cattle (excluding veal calves), swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight in divided doses for a maximum of 14 days. Dosage Schedule for treatment of colibacillosis: Pounds of Amount of Neomycin Liquid Body Weight Per Day in Divided Doses 25 lbs 1/4 teaspoonful 50 lbs 1/2 teaspoonful 100 lbs 1 teaspoonful 300 lbs 1 tablespoonful 600 lbs 1 fluid ounce Teaspoon = U.S. Standard Measure Neomycin Liquid may be given undiluted or diluted with water. Herd Treatment: Each bottle will treat 9,600 pounds body weight. Therefore, estimate the total number of pounds body weight of the animals to be treated and administer on (1) fluid ounce for each 600 pounds. The product should be added to the amount of drinking water to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) teaspoon in water or milk for each 100 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to be consumed in 12-24 hours.

ORAL

NEOMYCIN LIQUID

Administer to cattle, swine, sheep and goats at a dose of 10 mg neomycin sulfate per pound of body weight in divided doses for a maximum of 14 days. DOSAGE SCHEDULE FOR TREATMENT OF COLIBACILLOSIS: Amount of Neomycin Solution Pounds of body weight Per Day in Divided Doses 25 lbs 1/4 teaspoonful 50 lbs 1/2 teaspoonful 100 lbs 1 teaspoonful 300 lbs 1 tablespoonful 600 lbs 1 fluid ounce USE DIRECTION: Teaspoon = U.S. Standard Measure Neomycin Solution may be given undiluted or diluted with water. Herd Treatment: Each bottle will treat 76,800 pounds body weight. Therefore, estimate the total number of pounds body weight of the animals to be treate3d and administer one (1) fluid ounce for each 600 pounds. The product should be added to the amount of drinking water to be consumed in 12-24 hours. Provide medicated water as the sole source of water each day until consumed, followed by non-medicated water as required. Fresh medicated water should be prepared each day. Individual Animal Treatment: To provide 10 mg neomycin sulfate per pound of body weight, mix one (1) teaspoon in water or milk for each 100 pounds body weight. Administer daily either as a drench in divided doses or in the drinking water to consumed in 12-24 hours.

ORAL

Neovet

Frequency of administration is dependent on the severity of the condition. For mild inflammations, application may range from once daily to once a week; for severe conditions Animax Ointment may be applied as often as two to three times daily, if necessary. Frequency of treatment may be decreased as improvement occurs. Wear gloves during the administration of the ointment or wash hands immediately after application. Otitis Clean ear canal of impacted cerumen. Inspect canal and remove any foreign bodies such as grass awns, ticks, etc. Instill three to five drops of Animax Ointment. Preliminary use of a local anesthetic may be advisable. Infected Anal Glands, Cystic Areas, etc. Drain gland or cyst and then fill with Animax Ointment. Other Dermatologic Disorders Clean affected areas, removing any encrusted discharge or exudate. Apply Animax Ointment sparingly in a thin film.

TOPICAL, AURICULAR (OTIC)

Animax® Ointment (nystatin-neomycin sulfate-thiostrepton-triamcinolone acetonide ointment)

Prior to the administration of Dermatologic Solution TRESADERM, remove the ceruminous, purulent or foreign materials from the ear canal, as well as the crust which may be associated with dermatoses affecting other parts of the body. The design of the container nozzle safely allows partial insertion into the ear canal for ease of administration. The amount to apply and the frequency of treatment are dependent upon the severity and extent of the lesions. Five to 15 drops should be instilled in the ear twice daily. In treating dermatoses affecting other than the ear the surface of the lesions should be well moistened (2 to 4 drops per square inch) with Dermatologic Solution TRESADERM twice daily. The volume required will be dependent upon the size of the lesion. Application of TRESADERM should be limited to a period of not longer than one week.

TOPICAL

Tresaderm® (thiabendazole, dexamethasone, neomycin sulfate solution)

After cleansing the affected area, NEO-PREDEF with Tetracaine Powder is applied by compressing the sides of the container with short, sharp squeezes. In most instances a single daily application will be sufficient; however, it may be applied one to three times daily, as required.

TOPICAL

Neo-Predef® with Tetracaine Powder

In treating dermatoses affecting areas other than the ear, the surface of the lesions should be well moistened (2 to 4 drops per square inch) twice daily. In treating otitis externa, instill 5 to 15 drops in the ear twice daily. Treat for up to 7 days

Topical

Federal law restricts this drug to use by or on the order of a licensed veterinarian

Thiabendazole, Dexamethasone, Neomycin Sulfate Solution

DIRECTIONS: Use 1 level measure (included) to every 8 L (2 US gallons). Repeat every 7 days for up to 3 weeks or until symptoms disappear. Do not use UV, ozone, or chemical filtration during use. Remove with carbon before turning on UV.

ORAL

Neoplex™

Apply a thin film over the cornea 3 or 4 times daily

Ophthalmic

Federal law restricts this drug to use by or on the order of a licensed veterinarian

Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment